JPS58159443A - 芳香族アミン類の製造方法 - Google Patents

芳香族アミン類の製造方法

Info

Publication number: JPS58159443A
Authority: JP; Japan
Prior art keywords: catalyst; reaction; aromatic; hydrocarbons; gas
Prior art date: 1982-03-02
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP58029596A

Other languages

English (en)

Japanese (ja)

Inventor

ギユンタ−・シユタムマン

ロベルト・ベツカ−

ヨハン・グロ−リツヒ

ヘルム−ト・バルトマン

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer AG

Original Assignee

Bayer AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1982-03-02

Filing date

1983-02-25

Publication date

1983-09-21

1983-02-25 Application filed by Bayer AG filed Critical Bayer AG

1983-09-21 Publication of JPS58159443A publication Critical patent/JPS58159443A/ja

Status Pending legal-status Critical Current

Links

238000004519 manufacturing process Methods 0.000 title claims description 13
150000004982 aromatic amines Chemical class 0.000 title description 9
239000003054 catalyst Substances 0.000 claims description 67
238000000034 method Methods 0.000 claims description 65
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 60
150000002430 hydrocarbons Chemical class 0.000 claims description 54
229930195733 hydrocarbon Natural products 0.000 claims description 52
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 claims description 48
239000000203 mixture Substances 0.000 claims description 45
238000006243 chemical reaction Methods 0.000 claims description 36
-1 aromatic nitro compounds Chemical class 0.000 claims description 31
230000008569 process Effects 0.000 claims description 31
239000007789 gas Substances 0.000 claims description 30
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
239000004215 Carbon black (E152) Substances 0.000 claims description 21
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 21
229910002092 carbon dioxide Inorganic materials 0.000 claims description 11
238000011069 regeneration method Methods 0.000 claims description 11
239000001569 carbon dioxide Substances 0.000 claims description 10
230000008929 regeneration Effects 0.000 claims description 10
239000003345 natural gas Substances 0.000 claims description 9
230000000694 effects Effects 0.000 claims description 6
239000011541 reaction mixture Substances 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 4
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 3
238000010438 heat treatment Methods 0.000 claims description 3
239000003701 inert diluent Substances 0.000 claims description 3
150000003142 primary aromatic amines Chemical class 0.000 claims description 3
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239000010949 copper Substances 0.000 description 15
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238000004821 distillation Methods 0.000 description 6
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238000011282 treatment Methods 0.000 description 5
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229910052742 iron Inorganic materials 0.000 description 4
239000011593 sulfur Substances 0.000 description 4
QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical class [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 3
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RHQKKJPJCHGKQO-UHFFFAOYSA-N [Cu+2].[O-][Cr]([O-])=O Chemical class [Cu+2].[O-][Cr]([O-])=O RHQKKJPJCHGKQO-UHFFFAOYSA-N 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
230000003247 decreasing effect Effects 0.000 description 3
238000000605 extraction Methods 0.000 description 3
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239000007788 liquid Substances 0.000 description 3
239000007791 liquid phase Substances 0.000 description 3
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
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150000003839 salts Chemical class 0.000 description 3
239000010959 steel Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
241000894006 Bacteria Species 0.000 description 2
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
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WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
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YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
238000004380 ashing Methods 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
230000008901 benefit Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
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150000004649 carbonic acid derivatives Chemical class 0.000 description 2
238000010531 catalytic reduction reaction Methods 0.000 description 2
125000002091 cationic group Chemical group 0.000 description 2
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
239000004927 clay Substances 0.000 description 2
239000003245 coal Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
238000010586 diagram Methods 0.000 description 2
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
238000000921 elemental analysis Methods 0.000 description 2
239000011121 hardwood Substances 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
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239000004615 ingredient Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
239000000155 melt Substances 0.000 description 2
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VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 2
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
239000001294 propane Substances 0.000 description 2
229930195734 saturated hydrocarbon Natural products 0.000 description 2
238000000926 separation method Methods 0.000 description 2
SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
239000002689 soil Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 2
229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
238000005406 washing Methods 0.000 description 2
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
VNHGETRQQSYUGZ-UHFFFAOYSA-N 1-nitro-2-phenoxybenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1OC1=CC=CC=C1 VNHGETRQQSYUGZ-UHFFFAOYSA-N 0.000 description 1
YCANAXVBJKNANM-UHFFFAOYSA-N 1-nitroanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2[N+](=O)[O-] YCANAXVBJKNANM-UHFFFAOYSA-N 0.000 description 1
RJKGJBPXVHTNJL-UHFFFAOYSA-N 1-nitronaphthalene Chemical class C1=CC=C2C([N+](=O)[O-])=CC=CC2=C1 RJKGJBPXVHTNJL-UHFFFAOYSA-N 0.000 description 1
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ZGILLTVEEBNDOB-UHFFFAOYSA-N 2-chloro-5-nitrobenzonitrile Chemical compound [O-][N+](=O)C1=CC=C(Cl)C(C#N)=C1 ZGILLTVEEBNDOB-UHFFFAOYSA-N 0.000 description 1
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238000010521 absorption reaction Methods 0.000 description 1
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UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
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239000001034 iron oxide pigment Substances 0.000 description 1
VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
238000011031 large-scale manufacturing process Methods 0.000 description 1
239000003915 liquefied petroleum gas Substances 0.000 description 1
210000004072 lung Anatomy 0.000 description 1
229940093474 manganese carbonate Drugs 0.000 description 1
235000006748 manganese carbonate Nutrition 0.000 description 1
239000011656 manganese carbonate Substances 0.000 description 1
229910000016 manganese(II) carbonate Inorganic materials 0.000 description 1
XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
229940050176 methyl chloride Drugs 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000003801 milling Methods 0.000 description 1
238000000465 moulding Methods 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
229910017464 nitrogen compound Inorganic materials 0.000 description 1
150000002830 nitrogen compounds Chemical class 0.000 description 1
VLZLOWPYUQHHCG-UHFFFAOYSA-N nitromethylbenzene Chemical compound [O-][N+](=O)CC1=CC=CC=C1 VLZLOWPYUQHHCG-UHFFFAOYSA-N 0.000 description 1
150000002832 nitroso derivatives Chemical class 0.000 description 1
RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
229910052756 noble gas Inorganic materials 0.000 description 1
150000002835 noble gases Chemical class 0.000 description 1
ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 1
BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
150000003891 oxalate salts Chemical class 0.000 description 1
230000000803 paradoxical effect Effects 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
231100000572 poisoning Toxicity 0.000 description 1
230000000607 poisoning effect Effects 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000003361 porogen Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000003380 propellant Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
229910052705 radium Inorganic materials 0.000 description 1
HCWPIIXVSYCSAN-UHFFFAOYSA-N radium atom Chemical compound [Ra] HCWPIIXVSYCSAN-UHFFFAOYSA-N 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000003134 recirculating effect Effects 0.000 description 1
238000011084 recovery Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
238000006722 reduction reaction Methods 0.000 description 1
230000004044 response Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052709 silver Inorganic materials 0.000 description 1
239000004332 silver Substances 0.000 description 1
229910001961 silver nitrate Inorganic materials 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000011343 solid material Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
230000009469 supplementation Effects 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
229910052727 yttrium Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/30—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds
- C07C209/32—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds by reduction of nitro groups
- C07C209/325—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds by reduction of nitro groups reduction by other means than indicated in C07C209/34 or C07C209/36

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

JP58029596A 1982-03-02 1983-02-25 芳香族アミン類の製造方法 Pending JPS58159443A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19823207475 DE3207475A1 (de)	1982-03-02	1982-03-02	Verfahren zur herstellung von aromatischen aminen
DE32074751		1982-03-02

Publications (1)

Publication Number	Publication Date
JPS58159443A true JPS58159443A (ja)	1983-09-21

Family

ID=6157109

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP58029596A Pending JPS58159443A (ja)	1982-03-02	1983-02-25	芳香族アミン類の製造方法

Country Status (3)

Country	Link
EP (1)	EP0087690B1 (fr)
JP (1)	JPS58159443A (fr)
DE (2)	DE3207475A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2009514805A (ja) *	2005-10-10	2009-04-09	フェアストックテクノロジーズコーポレイション	液化金属合金を使用して有機化合物を変換するための方法および関連装置

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3641500A1 (de) *	1986-12-04	1988-06-16	Basf Ag	Verfahren zur reduktion von aromatischen verbindungen mit no-doppelbindungen
US4929737A (en) *	1988-02-03	1990-05-29	Eastman Kodak Company	Hydrogenation of halonitroaromatic compounds
RU2135460C1 (ru) *	1997-12-16	1999-08-27	Батрин Юрий Дмитриевич	Совместное получение анилина и n-метиланилина
RU2135461C1 (ru) *	1998-12-04	1999-08-27	Якушкин Михаил Иванович	Способ получения анилина
RU2136654C1 (ru) *	1998-12-04	1999-09-10	Якушкин Михаил Иванович	Способ получения анилина
RU2259350C2 (ru) *	2003-07-14	2005-08-27	Открытое акционерное общество "Пигмент"	Способ получения анилина и/или n-метиланилина и катализатор для него
RU2275353C2 (ru) *	2004-03-15	2006-04-27	Открытое акционерное общество "Пигмент"	Способ получения n-метиланилина
RU2270187C2 (ru) *	2004-04-14	2006-02-20	Валерий Александрович Головачев	Способ получения n-метиланилина

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3504035A (en) *	1966-07-01	1970-03-31	American Cyanamid Co	Process for preparing aromatic amines from aromatic nitro compounds

1982
- 1982-03-02 DE DE19823207475 patent/DE3207475A1/de not_active Withdrawn
1983
- 1983-02-18 EP EP83101551A patent/EP0087690B1/fr not_active Expired
- 1983-02-18 DE DE8383101551T patent/DE3360009D1/de not_active Expired
- 1983-02-25 JP JP58029596A patent/JPS58159443A/ja active Pending

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2009514805A (ja) *	2005-10-10	2009-04-09	フェアストックテクノロジーズコーポレイション	液化金属合金を使用して有機化合物を変換するための方法および関連装置

Also Published As

Publication number	Publication date
DE3360009D1 (en)	1984-12-06
EP0087690B1 (fr)	1984-10-31
DE3207475A1 (de)	1983-09-15
EP0087690A1 (fr)	1983-09-07

Publication	Publication Date	Title
JPS6038380B2 (ja)	1985-08-31	接触アミノ化法
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US4083809A (en)	1978-04-11	Hydrogenation catalyst and method of producing same
TWI377188B (en)	2012-11-21	Method of converting c9 aromatics-comprising mixtures to xylene isomers
US3966833A (en)	1976-06-29	Process for hydrodealkylating alkylaromatic hydrocarbons
AU2009235497B2 (en)	2013-11-14	Method for the dehydroaromatisation of mixtures containing methane by regenerating the corresponding catalysts that are devoid of precious metal
JP2577830B2 (ja)	1997-02-05	脱水素および、または脱水素環化用触媒組成物およびその使用方法
JPH01252695A (ja)	1989-10-09	単一触媒系を用いた酸化的再加熱を伴うスチーム脱水素法
JPS58159443A (ja)	1983-09-21	芳香族アミン類の製造方法
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IE47477B1 (en)	1984-03-21	Process for the dehalogenation of halogen-containing aromatic amines
WO2005037962A1 (fr)	2005-04-28	Procede de production de gaz de petrole liquefie contenant du propane ou du butane comme composant principal
WO2005066112A1 (fr)	2005-07-21	Procede pour la reduction catalytique d'amides
WO1989000452A1 (fr)	1989-01-26	Composition catalytique et procede permettant la deshydrogenation selective
JPS5933234A (ja)	1984-02-23	脱水素可能な炭化水素の脱水素方法
US2590124A (en)	1952-03-25	Partial oxidation of hydrocarbons using gaseous sulfur trioxide
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JPS6256788B2 (fr)	1987-11-27
US2725401A (en)	1955-11-29	Synthesis of oxygenated organic compounds
US4523016A (en)	1985-06-11	Process for the catalytic dehydrogenation of piperidine
JPS58225078A (ja)	1983-12-27	モルホリン製造用触媒
KR100588948B1 (ko)	2006-06-14	디메틸에테르 제조용 촉매, 이의 제조방법 및 이를 이용한디메틸에테르 제조방법

JPS58159443A - 芳香族アミン類の製造方法 - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (2)

Publications (1)

Family

ID=6157109

Family Applications (1)

Country Status (3)

Cited By (1)

Families Citing this family (8)

Family Cites Families (1)

Cited By (1)

Also Published As

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